| Literature DB >> 25486132 |
Lesley-Ann Sutton1, Giorgos Papadopoulos2, Anastasia Hadzidimitriou1,3, Stavros Papadopoulos2, Efterpi Kostareli4, Richard Rosenquist1, Dimitrios Tzovaras2, Kostas Stamatopoulos1,3,5.
Abstract
Patients with chronic lymphocytic leukemia (CLL) assigned to stereotyped subset #4 express highly homologous B-cell receptor immunoglobulin (BcR IG) sequences with intense intraclonal diversification (ID) in the context of ongoing somatic hypermutation (SHM). Their remarkable biological and clinical similarities strongly support derivation from a common ancestor. We here revisited ID in subset #4 CLL to reconstruct their evolutionary history as a community of related clones. To this end, using specialized bioinformatics tools we assessed both IGHV-IGHD-IGHJ rearrangements (n = 511) and IGKV-IGKJ rearrangements (n = 397) derived from eight subset #4 cases. Due to high sequence relatedness, a number of subclonal clusters from different cases lay very close to one another, forming a core from which clusters exhibiting greater variation stemmed. Minor subclones from individual cases were mutated to such an extent that they now resembled the sequences of another patient. Viewing the entire subset #4 data set as a single entity branching through diversification enabled inference of a common sequence representing the putative ancestral BcR IG expressed by their still elusive common progenitor. These results have implications for improved understanding of the ontogeny of CLL subset #4, as well as the design of studies concerning the antigenic specificity of the clonotypic BcR IGs.Entities:
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Year: 2015 PMID: 25486132 PMCID: PMC4398667 DOI: 10.2119/molmed.2014.00140
Source DB: PubMed Journal: Mol Med ISSN: 1076-1551 Impact factor: 6.354